Device recall
Z-2339-2008: Sunrise Medical Quickie Groove Power Wheelchair with Transit option The product…
FDA device recall · Class II · Sunrise Medical Inc
Key facts
| Recall number (Z-number) | Z-2339-2008 |
|---|---|
| Recall event | 48662 |
| Product | Sunrise Medical Quickie Groove Power Wheelchair with Transit option The product is a powered wheelchair for human use. |
| Product code | ITI |
| Recalling firm | Sunrise Medical Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 22, 2009 |
| 510(k) numbers | K060531 |
| FEI number | 2937137 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database